PMDA drug package insert
ドセタキセル点滴静注20mg/1mL「ニプロ」
PMDA Prescription drug · ニプロ株式会社 · package insert Jun 19, 2026
Key facts
| Brand names | ドセタキセル点滴静注20mg/1mL「ニプロ」, ドセタキセル点滴静注80mg/4mL「ニプロ」 |
|---|---|
| Nonproprietary names | ドセタキセル |
| Companies | 製造販売元／ニプロ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | タキソイド系抗悪性腫瘍剤 |
| Therapeutic category codes | 87424 |
| YJ codes | 4240405A3102, 4240405A4109 |
| Approval numbers | 22700AMX00434, 22700AMX00435 |
| Package insert edition | 第3版 |
| Package insert date | Jun 19, 2026 |
| PMDA document key | 530100_4240405A3102_1 |
| PMDA company code | 530100 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None Safety communications
- No PMDA review report published
- No Risk management plan (RMP)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMDA approved drugs and package inserts (Japan)
Japan's PMDA publishes the package insert (添付文書) of every prescription drug, OTC drug and regenerative medical product, with brand and nonproprietary names, YJ codes and approval numbers. Names appear in Japanese as published.
Source: Pharmaceuticals and Medical Devices Agency (PMDA), Japan, package insert database · Source date: